FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SAS(TM) MONOCLONAL HCG-SLIDE

K Number: K930609 · Decision Mar 29, 1993
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
95
Applicant Total
199
Review Days
52

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Basic Information

Device Name
SAS(TM) MONOCLONAL HCG-SLIDE
K Number
K930609
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sa Scientific, Inc.
Date Received
February 5, 1993
Decision Date
March 29, 1993
Product Code
JHJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JHJ Agglutination Method, Human Chorionic Gonadotropin

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Other Clearances by Sa Scientific, Inc.

K Number Device Name
K100227 SAS FLUALERT A&B, SAS INFLUENZA A TEST
K080380 SAS INFLUENZA A & B TEST
K041439 SAS INFLUENZA B TEST
K041441 SAS INFLUENZA A TEST
K030628 SAS RSV CONTROL KIT
K022845 SAS RSV TEST
K022683 SAS BLOOD/SERUM/URINE/URINE HCG
K023270 SAS STREPALERT
K020438 SAS VALUE HCG
K013379 SAS STREPALERT
Search all 199 clearances from Sa Scientific, Inc. →